ClinVar Miner

List of variants in gene combination A2M, KLRG1 reported as uncertain significance by Ambry Genetics

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Gene type:
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Total variants: 97
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HGVS dbSNP gnomAD frequency
NM_000014.6(A2M):c.3829C>A (p.Gln1277Lys) rs372114265 0.00017
NM_000014.6(A2M):c.3008A>C (p.Lys1003Thr) rs776483113 0.00011
NM_000014.6(A2M):c.896G>A (p.Cys299Tyr) rs750697212 0.00011
NM_000014.6(A2M):c.4118G>A (p.Arg1373His) rs201692842 0.00009
NM_000014.6(A2M):c.4033G>A (p.Val1345Met) rs372632979 0.00008
NM_000014.6(A2M):c.1202A>C (p.Glu401Ala) rs367610653 0.00005
NM_000014.6(A2M):c.1760T>C (p.Val587Ala) rs146966573 0.00004
NM_000014.6(A2M):c.3014T>C (p.Ile1005Thr) rs558034541 0.00004
NM_000014.6(A2M):c.1402C>A (p.Leu468Ile) rs202178042 0.00003
NM_000014.6(A2M):c.3653C>T (p.Thr1218Met) rs769739191 0.00003
NM_000014.6(A2M):c.4364C>T (p.Thr1455Met) rs376343602 0.00003
NM_000014.6(A2M):c.1205A>G (p.His402Arg) rs375282521 0.00002
NM_000014.6(A2M):c.2411G>A (p.Arg804His) rs117138141 0.00002
NM_000014.6(A2M):c.260T>A (p.Val87Asp) rs776923281 0.00002
NM_000014.6(A2M):c.313G>C (p.Val105Leu) rs759883074 0.00002
NM_000014.6(A2M):c.322A>G (p.Lys108Glu) rs1329637882 0.00002
NM_000014.6(A2M):c.1096T>C (p.Phe366Leu) rs751910472 0.00001
NM_000014.6(A2M):c.1235C>T (p.Thr412Ile) rs1482300294 0.00001
NM_000014.6(A2M):c.1735C>G (p.Pro579Ala) rs374437029 0.00001
NM_000014.6(A2M):c.1846T>C (p.Ser616Pro) rs955281793 0.00001
NM_000014.6(A2M):c.2286C>G (p.Ile762Met) rs369403894 0.00001
NM_000014.6(A2M):c.2330G>A (p.Gly777Glu) rs975545965 0.00001
NM_000014.6(A2M):c.2390C>T (p.Thr797Ile) rs779160830 0.00001
NM_000014.6(A2M):c.2785G>C (p.Glu929Gln) rs1359556241 0.00001
NM_000014.6(A2M):c.2962G>A (p.Asp988Asn) rs768021420 0.00001
NM_000014.6(A2M):c.3385G>A (p.Glu1129Lys) rs1211762376 0.00001
NM_000014.6(A2M):c.3656C>A (p.Ala1219Asp) rs776551974 0.00001
NM_000014.6(A2M):c.3674C>T (p.Ser1225Leu) rs771531434 0.00001
NM_000014.6(A2M):c.4205C>G (p.Ser1402Cys) rs1300462625 0.00001
NM_000014.6(A2M):c.4264G>A (p.Val1422Met) rs754217279 0.00001
NM_000014.6(A2M):c.542T>C (p.Phe181Ser) rs1042685386 0.00001
NM_000014.6(A2M):c.1108C>T (p.Arg370Cys)
NM_000014.6(A2M):c.1192A>G (p.Thr398Ala) rs2498287656
NM_000014.6(A2M):c.1225A>G (p.Ile409Val)
NM_000014.6(A2M):c.1231A>G (p.Thr411Ala) rs2498287146
NM_000014.6(A2M):c.124G>A (p.Glu42Lys)
NM_000014.6(A2M):c.1340C>G (p.Thr447Ser)
NM_000014.6(A2M):c.1360C>T (p.Pro454Ser) rs2498266900
NM_000014.6(A2M):c.1373T>G (p.Phe458Cys) rs752422412
NM_000014.6(A2M):c.1456A>T (p.Thr486Ser)
NM_000014.6(A2M):c.1616G>A (p.Arg539Gln)
NM_000014.6(A2M):c.1628A>G (p.Tyr543Cys)
NM_000014.6(A2M):c.1747G>A (p.Ala583Thr)
NM_000014.6(A2M):c.1771C>T (p.Pro591Ser)
NM_000014.6(A2M):c.1841C>T (p.Ser614Leu)
NM_000014.6(A2M):c.1844C>T (p.Ala615Val) rs1017971143
NM_000014.6(A2M):c.1868C>G (p.Pro623Arg) rs2498210774
NM_000014.6(A2M):c.1946A>G (p.Tyr649Cys)
NM_000014.6(A2M):c.1961C>G (p.Thr654Arg)
NM_000014.6(A2M):c.1991A>G (p.Lys664Arg)
NM_000014.6(A2M):c.1997T>C (p.Met666Thr)
NM_000014.6(A2M):c.2003G>A (p.Ser668Asn) rs773788913
NM_000014.6(A2M):c.2039A>G (p.Asn680Ser) rs1705513693
NM_000014.6(A2M):c.214A>C (p.Ser72Arg) rs2498376711
NM_000014.6(A2M):c.2177C>T (p.Pro726Leu)
NM_000014.6(A2M):c.2201A>T (p.Tyr734Phe)
NM_000014.6(A2M):c.2251G>C (p.Val751Leu) rs2498168411
NM_000014.6(A2M):c.2380G>T (p.Val794Leu)
NM_000014.6(A2M):c.240G>C (p.Glu80Asp)
NM_000014.6(A2M):c.2491T>C (p.Ser831Pro) rs2498157048
NM_000014.6(A2M):c.2601T>G (p.Asn867Lys) rs1949161329
NM_000014.6(A2M):c.2689G>T (p.Asp897Tyr) rs1358336887
NM_000014.6(A2M):c.2702A>C (p.Lys901Thr)
NM_000014.6(A2M):c.278A>T (p.Lys93Met) rs754940338
NM_000014.6(A2M):c.2809C>T (p.Pro937Ser)
NM_000014.6(A2M):c.3013A>G (p.Ile1005Val)
NM_000014.6(A2M):c.3053A>G (p.Tyr1018Cys)
NM_000014.6(A2M):c.3299C>A (p.Thr1100Asn) rs1219589381
NM_000014.6(A2M):c.3326T>G (p.Leu1109Arg)
NM_000014.6(A2M):c.3349A>C (p.Thr1117Pro)
NM_000014.6(A2M):c.3364C>T (p.Arg1122Cys)
NM_000014.6(A2M):c.3488G>C (p.Arg1163Thr) rs2498029321
NM_000014.6(A2M):c.350G>T (p.Arg117Leu) rs772340371
NM_000014.6(A2M):c.3521C>G (p.Ala1174Gly)
NM_000014.6(A2M):c.3593A>T (p.Glu1198Val) rs1486214613
NM_000014.6(A2M):c.3776A>C (p.His1259Pro)
NM_000014.6(A2M):c.381T>A (p.Ser127Arg)
NM_000014.6(A2M):c.3967T>C (p.Tyr1323His)
NM_000014.6(A2M):c.4040C>T (p.Thr1347Ile)
NM_000014.6(A2M):c.4045C>T (p.Pro1349Ser)
NM_000014.6(A2M):c.4057G>C (p.Asp1353His) rs2497987448
NM_000014.6(A2M):c.4066A>G (p.Lys1356Glu) rs1163589028
NM_000014.6(A2M):c.4204T>G (p.Ser1402Ala) rs2497962698
NM_000014.6(A2M):c.4232G>A (p.Ser1411Asn)
NM_000014.6(A2M):c.4379T>C (p.Ile1460Thr)
NM_000014.6(A2M):c.4399T>G (p.Cys1467Gly) rs2497943953
NM_000014.6(A2M):c.445G>A (p.Val149Ile)
NM_000014.6(A2M):c.479A>T (p.Glu160Val)
NM_000014.6(A2M):c.490C>G (p.Leu164Val) rs2498346347
NM_000014.6(A2M):c.521G>A (p.Arg174His) rs369574498
NM_000014.6(A2M):c.616G>T (p.Val206Leu) rs750530590
NM_000014.6(A2M):c.622C>G (p.Gln208Glu) rs1938594832
NM_000014.6(A2M):c.703G>T (p.Val235Leu)
NM_000014.6(A2M):c.721A>G (p.Ile241Val)
NM_000014.6(A2M):c.733G>A (p.Glu245Lys)
NM_000014.6(A2M):c.838G>A (p.Gly280Ser)
NM_000014.6(A2M):c.98T>C (p.Val33Ala) rs2498378353

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